3-ethyl-2‐(1-(4-(trifluoromethoxy)benzyl)‐1H-pyrazol-4-yl)quinolin‐4(1H)‐one

Base Information

• Chemical Name: 3-ethyl-2‐(1-(4-(trifluoromethoxy)benzyl)‐1H-pyrazol-4-yl)quinolin‐4(1H)‐one
• CAS No.: 1379615-43-6
• Molecular Formula: C₂₂H₁₈F₃N₃O₂
• Molecular Weight: 413.399
• Mol file: 1379615-43-6.mol

Synonyms:3-ethyl-2‐(1-(4-(trifluoromethoxy)benzyl)‐1H-pyrazol-4-yl)quinolin‐4(1H)‐one

Chemical Property of 3-ethyl-2‐(1-(4-(trifluoromethoxy)benzyl)‐1H-pyrazol-4-yl)quinolin‐4(1H)‐one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-ethyl-2‐(1-(4-(trifluoromethoxy)benzyl)‐1H-pyrazol-4-yl)quinolin‐4(1H)‐one

There total 4 articles about 3-ethyl-2‐(1-(4-(trifluoromethoxy)benzyl)‐1H-pyrazol-4-yl)quinolin‐4(1H)‐one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 65.0%

2-(2'-anilinyl)-4,4-dimethyl-4,5-dihydro-1,3-oxazole (63478-10-4) + 1-(1‐(4-(trifluoromethoxy)benzyl)-1H-‐pyrazol-4‐yl)butan-1-one (1379615-67-4) → 3-ethyl-2‐(1-(4-(trifluoromethoxy)benzyl)‐1H-pyrazol-4-yl)quinolin‐4(1H)‐one (1379615-43-6)

Guidance literature:

With trifluorormethanesulfonic acid; In butan-1-ol; Reflux;

DOI:10.1021/acsmedchemlett.8b00371

Reference yield: 65.0%

→ 3-ethyl-2‐(1-(4-(trifluoromethoxy)benzyl)‐1H-pyrazol-4-yl)quinolin‐4(1H)‐one (1379615-43-6)

Guidance literature:

Reference yield:

4-trifluoromethoxybenzyl bromide (50824-05-0) → 3-ethyl-2‐(1-(4-(trifluoromethoxy)benzyl)‐1H-pyrazol-4-yl)quinolin‐4(1H)‐one (1379615-43-6)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / acetone / 3 h / Reflux

2: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 1,3-bis-(diphenylphosphino)propane; pyrrolidine / N,N-dimethyl-formamide / 6 h / 110 °C / Molecular sieve; Inert atmosphere

3: trifluorormethanesulfonic acid / butan-1-ol / Reflux

With pyrrolidine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; trifluorormethanesulfonic acid; 1,3-bis-(diphenylphosphino)propane; potassium carbonate; In N,N-dimethyl-formamide; acetone; butan-1-ol;

DOI:10.1021/acsmedchemlett.8b00371

upstream raw materials:

4-trifluoromethoxybenzyl bromide

4-iodo‐1-(4‐(trifluoromethoxy)benzyl)-1H‐pyrazole

2-(2'-anilinyl)-4,4-dimethyl-4,5-dihydro-1,3-oxazole

1-(1‐(4-(trifluoromethoxy)benzyl)-1H-‐pyrazol-4‐yl)butan-1-one